US4770889A - Sweetener - Google Patents
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- Publication number
- US4770889A US4770889A US07/026,306 US2630687A US4770889A US 4770889 A US4770889 A US 4770889A US 2630687 A US2630687 A US 2630687A US 4770889 A US4770889 A US 4770889A
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- US
- United States
- Prior art keywords
- sweetness
- aspartame
- alcohols
- sweetener
- sorbitol
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/60—Sweeteners
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/346—Finished or semi-finished products in the form of powders, paste or liquids
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/31—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives
- A23L27/32—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives containing dipeptides or derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/33—Artificial sweetening agents containing sugars or derivatives
- A23L27/34—Sugar alcohols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G2200/00—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents
- A23G2200/06—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents containing beet sugar or cane sugar if specifically mentioned or containing other carbohydrates, e.g. starches, gums, alcohol sugar, polysaccharides, dextrin or containing high or low amount of carbohydrate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S426/00—Food or edible material: processes, compositions, and products
- Y10S426/804—Low calorie, low sodium or hypoallergic
Definitions
- the present invention relates to a sweetener or a sweetened food which comprises aspartame. More particularly, it relates to a sweetener or a sweetened food which comprises aspartame and sugar alcohols.
- aspartame is characterized as a sweetener possessing a clear pleasant sweetness and is free from bitter aftertaste. It is however undeniable that the sweetness of aspartame is not satisfactorily rich in mouthfulness, and that it has a tendency to leave a lingering taste characteristic of sweetening agents having a high sweetening potency.
- aspartame characteristics of aspartame are recognized not only in cases where it is used alone but also in cases where it is used in combination with other flavoring or fragrant substances.
- such characteristics tend to be strengthened when it is added as a table sweetener to coffee, tea, etc., or when it is incorporated into such beverages as soda pops and carbonated cola beverages, of which sweetness and fragrance are directly tasted.
- aspartame has hitherto been used in combination with various substances, including, e.g., aluminum sulfate and potassium naringin [Japanese Patent Application (Laid Open) No. 90,667/77]; sodium L-glutamate [Japanese Patent Application (Laid Open) No. 148,255/81]; glycine, alanine and serine [Japanese Patent Application (Laid Open) No. 63,068/82]; sucrose [Japanese Patent Application (Laid Open) No. 155,965/82]; L-ascorbic acid [Japanese Patent Application (Laid Open) Nos.
- a sweetener or a sweetened food comprising, in addition to aspartame, (1) sorbitol, (2) maltitol and (3) "other oligosugar alcohols" in the following ratio:
- oligosugar alcohols there can be used sugar alcohols containing more than 2 sugar units. It is preferable to use a mixture of oligosugar alcohols consisting of 50 to 60% of sugar alcohols containing 3 to 6 sugar units and 40 to 50% of sugar alcohols containing more than 6 sugar units.
- sorbitol When used in combination with aspartame, sorbitol is capable of imparting an agreeable initial taste, and "other oligosugar alcohols" are capable of enriching the sweetness of aspartame.
- these effect are not at all strong.
- maltitol exhibits little effects on the improvement of the sweetness of aspartame when it is used alone. In spite of these facts, maltitol is capable of improving the sweetness of aspartame when used in combination with sorbitol and "other oligosugar alcohols" in particular ratios.
- sorbitol, maltitol and “other sugar alcohols” are little or only sightly effective in improvement of the quality of sweetness of aspartame when they are used individually, but the sweetness of aspartame can be markedly improved by using the three components together with aspartame in particular ratios described hereinabove.
- the ratio of sorbitol to the total weight of the sugar alcohols is less than 1%, the initial taste of the resulting sweetener becomes insufficient.
- the resulting sweetener lacks the rich sweetness of aspartame.
- the content of sorbitol exceeds 10% by weight or the content of "other oligosugar alcohols” exceeds 55% by weight, the desired synergistic improvements in the quality of sweetness of aspartame could not be fully attained because of the lowering of the maltitol content. Accordingly, these three components must be contained in the following percentage (based on the total weight of sugar alcohols): sorbitol, 1 to 10%; maltitol, 45 to 55%; and "other oligosugar alcohols", 35 to 55%.
- the sugar alcohols are used in such an amount that the ratio of the combined sweetness of the sugar alcohols to aspartame is in the range of 0.5:9.5 to 3:7.
- the ratio is 0.5 or less, the quality of the sweetness of aspartame could not be improved substantially.
- it is more than 7, the clear and sharp sweetness characteristic of aspartame disappears and an undesirably flat sweetness results.
- the sweetener according to the present invention can be in various forms, including liquid, tablets, granules, powders, etc.
- the sweetened food according to the present invention can be in the form of beverages, frozen sweets, cookies, fermented milks, and the like. There are no particular limitations on the forms of the sweetener and the kinds of the sweetened food.
- the present invention can be particularly useful as table sugars and beverages, including soft drinks, such as carbonated flavored beverages (e.g., soda pops, cola beverages, etc.), juice-containing beverages and artificial fruit-flavored beverages; lactic acid beverages; lactobacillus-containing beverages; and the like.
- synergistic effects of the present invention can be markedly exhibited in carbonated flavored beverages, such as soda pops and carbonated cola beverages, which do not contain such taste-imparting ingredients as juice and lactic acid, and the taste of which is composed only of such ingredients as organic acids and aspartame.
- the sweetener or sweetened food of the present invention can be used together with other ordinary raw food materials, and there are no particular restrictions on the methods to be employed for their production.
- the concentration of aspartame and the sugar alcohols to be contained in the sweetener or sweetened food is not limited to any particular range. It can however be generally preferable to use aspartame at a concentration of 0.01 to 0.05 g/dl and the sugar alcohols at a concentration of 1 to 20 g/dl. When aspartame is used at a concentration less than 0.01 g/dl, the desired effects of the present invention may not be attained, depending on the kinds and concentrations of other ingredients contained therein.
- a sweetener or a sweetened food having a sweetness which is very similar to that of sucrose with regard to initial taste, richness, sustainability and aftertaste.
- the overall rating of the aqueous sucrose solution was 7.2.
- the "other oligosugar alcohols (HG 3 and above)" used in the above test was obtained by reducing dextrin having a DE value of about 20 and then recovering fractions of HG 3 and above by column chromatography.
- composition of the oligosugar alcohols recovered by the column chromatography was analysed by high pressure liquid chromatography (HPLC). The following results were obtained: Content of HG 3 to HG 9 components, 72%; and content of the components of HG 10 and above, 28%.
- the carbonated lemon lime beverages obtained were evaluated by a sensory test performed by a panel of 10 members in accordance with the two point comparison method, using Control Sample 1 (sucrose-containing sample) as a control. Results obtained are shown in Table 4.
- Granules of table sweeteners were prepared from the ingredients shown in Table 5, thereby using water as a binder.
- the product according to the invention had a sweetness degree of 4 (i.e., the sweetness of 1 g of the product according to the invention corresponded to that of 4 g of sucrose).
- the two kinds of sugar granules obtained were separately added to coffee, tea, and plain yoghurt in an amount of 1.5 g/100 ml each and evaluated by a sensory test of a panel of 15 members using sucrose as a control. Results obtained are shown in Table 6.
- the sugar alcohols according to the present invention can be heated before being admixed with aspartame.
- a liquid sweetener is capable of maintaining a high concentration of aspartame even after being cooled to room temperature and, therefore, possesses a strong sweetness of superior quality.
- the sugar alcohols can be preheated to a temperature of 50° to 110° C., preferably 60° to 90° C. When the temperature is lower than 50° C., part of aspartame may remain undissolved, and when it is above 110° C., decomposition of aspartame may take place.
- the concentration of aspartame in said liquid sweetener can be preferably from 0.3% by weight (degree of sweetness: ca. 1.0) to 0.8% by weight (degree of sweetness: ca. 2.0). When it is less than 0.3% by weight, there may be caused diarrhea, and when it is more than 0.8% by weight, an inferior quality of sweetness may result.
- the sweetener or sweetened food of the present invention can be additionally incorporated with sodium salts of organic acids, such as sodium tartrate, sodium malate and sodium citrate.
- organic acid salts can be used in an amount of from 30 to 300% by weight, preferably from 30 to 200% by weight.
- a liquid sweetener (A) was prepared from the following ingredients.
- the sugar alcohols were heated to about 80° C. and admixed with aspartame and sodium tartrate by using a mixer.
- liquid sweetener was clear. When added to coffee and tea, the sweetener was capable of imparting a satisfactory sweetness to both of them.
- a liquid sweetner (B) was prepared from the above ingredients in the same manner as in Example 4, except that the sugar alcohols were heated to a temperature of about 90° C. before being admixed. When this sweetener was allowed to stand at room temperature, there was formed a small amount of precipitate or gel of aspartame. However, it was usable as a liquid sweetener in either case. When added to coffee, the sweetener gave a satisfactory sweetness to the coffee as in the case of Example 4.
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
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Abstract
Sweetners and sweetened foods are disclosed which comprise aspartame (APM) and sugar alcohols in the following ratio:
______________________________________
(1) Sorbitol 1 to 10 wt %
(2) Martitol 45 to 55 wt %
(3) Other oligosugar alcohols
35 to 55 wt %
(4) Ratio of sweetness
APM:Sugar alcohols (1)-(3) =
9.5:0.5 to 3:7
______________________________________
The sweeteners and sweetened foods can be table sugars, frozen sweets, cookies, fermented milks or beverages, such as soda pops and carbonated cola drinks, and have a sweetness similar to sucrose.
Description
1. Field of the Invention
The present invention relates to a sweetener or a sweetened food which comprises aspartame. More particularly, it relates to a sweetener or a sweetened food which comprises aspartame and sugar alcohols.
2. Description of the Prior Art
Of known low caloric sweetening agents, aspartame is characterized as a sweetener possessing a clear pleasant sweetness and is free from bitter aftertaste. It is however undeniable that the sweetness of aspartame is not satisfactorily rich in mouthfulness, and that it has a tendency to leave a lingering taste characteristic of sweetening agents having a high sweetening potency.
Such characteristics of aspartame are recognized not only in cases where it is used alone but also in cases where it is used in combination with other flavoring or fragrant substances. In particular, such characteristics tend to be strengthened when it is added as a table sweetener to coffee, tea, etc., or when it is incorporated into such beverages as soda pops and carbonated cola beverages, of which sweetness and fragrance are directly tasted.
In order to improve the quality of its sweetness, aspartame has hitherto been used in combination with various substances, including, e.g., aluminum sulfate and potassium naringin [Japanese Patent Application (Laid Open) No. 90,667/77]; sodium L-glutamate [Japanese Patent Application (Laid Open) No. 148,255/81]; glycine, alanine and serine [Japanese Patent Application (Laid Open) No. 63,068/82]; sucrose [Japanese Patent Application (Laid Open) No. 155,965/82]; L-ascorbic acid [Japanese Patent Application (Laid Open) Nos. 141,760/83 and 19,474/85]; starch syrup, dextrin and glucose [Japanese Patent Application (Laid Open) Nos. 114,167/85, 114,169/85 and 114,168/85]; and the like.
However, it could hardly be said that these prior arts have fully succeeded in improving the sweetness of beverages, etc. to a level comparable to sucrose.
It is therefore an object of the present invention to provide a sweetener or a sweetened food which is free from the above disadvantages of aspartame.
It is another object of the present invention to provide a sweetener, in particular, table sugar having a mild and pleasant sweetness comparable to sucrose.
It is a further object of the present invention to provide a food, in particular, a carbonated beverage imparted with sweetness which is not disagreeable to consumers accustomed to the taste of sucrose.
Other objects of the present invention will become apparent from the following description.
In view of the above, the inventors have conducted intensive investigations for the improvement of the quality of sweetness of aspartame. As a result, it has now been found that the sweetness of aspartame can be markedly improved by using aspartame in combination with sugar alcohols in particular ratios.
Accordingly, there is provided by the present invention a sweetener or a sweetened food comprising, in addition to aspartame, (1) sorbitol, (2) maltitol and (3) "other oligosugar alcohols" in the following ratio:
______________________________________
(1) Sorbitol 1 to 10%
(2) Maltitol 45 to 55%
(3) "Other oligosugar alcohols"
35 to 55%
______________________________________
As "other oligosugar alcohols", there can be used sugar alcohols containing more than 2 sugar units. It is preferable to use a mixture of oligosugar alcohols consisting of 50 to 60% of sugar alcohols containing 3 to 6 sugar units and 40 to 50% of sugar alcohols containing more than 6 sugar units.
When used in combination with aspartame, sorbitol is capable of imparting an agreeable initial taste, and "other oligosugar alcohols" are capable of enriching the sweetness of aspartame. However, these effect are not at all strong. On the other hand, maltitol exhibits little effects on the improvement of the sweetness of aspartame when it is used alone. In spite of these facts, maltitol is capable of improving the sweetness of aspartame when used in combination with sorbitol and "other oligosugar alcohols" in particular ratios. That is to say, sorbitol, maltitol and "other sugar alcohols" are little or only sightly effective in improvement of the quality of sweetness of aspartame when they are used individually, but the sweetness of aspartame can be markedly improved by using the three components together with aspartame in particular ratios described hereinabove.
If the ratio of sorbitol to the total weight of the sugar alcohols is less than 1%, the initial taste of the resulting sweetener becomes insufficient. When said "other oligosugar alcohols" are contained therein in an amount of less than 35% by weight, the resulting sweetener lacks the rich sweetness of aspartame. On the other hand, if the content of sorbitol exceeds 10% by weight or the content of "other oligosugar alcohols" exceeds 55% by weight, the desired synergistic improvements in the quality of sweetness of aspartame could not be fully attained because of the lowering of the maltitol content. Accordingly, these three components must be contained in the following percentage (based on the total weight of sugar alcohols): sorbitol, 1 to 10%; maltitol, 45 to 55%; and "other oligosugar alcohols", 35 to 55%.
The sugar alcohols are used in such an amount that the ratio of the combined sweetness of the sugar alcohols to aspartame is in the range of 0.5:9.5 to 3:7. When the ratio is 0.5 or less, the quality of the sweetness of aspartame could not be improved substantially. When it is more than 7, the clear and sharp sweetness characteristic of aspartame disappears and an undesirably flat sweetness results.
The sweetener according to the present invention can be in various forms, including liquid, tablets, granules, powders, etc. The sweetened food according to the present invention can be in the form of beverages, frozen sweets, cookies, fermented milks, and the like. There are no particular limitations on the forms of the sweetener and the kinds of the sweetened food. The present invention can be particularly useful as table sugars and beverages, including soft drinks, such as carbonated flavored beverages (e.g., soda pops, cola beverages, etc.), juice-containing beverages and artificial fruit-flavored beverages; lactic acid beverages; lactobacillus-containing beverages; and the like. The synergistic effects of the present invention can be markedly exhibited in carbonated flavored beverages, such as soda pops and carbonated cola beverages, which do not contain such taste-imparting ingredients as juice and lactic acid, and the taste of which is composed only of such ingredients as organic acids and aspartame.
The sweetener or sweetened food of the present invention can be used together with other ordinary raw food materials, and there are no particular restrictions on the methods to be employed for their production. The concentration of aspartame and the sugar alcohols to be contained in the sweetener or sweetened food is not limited to any particular range. It can however be generally preferable to use aspartame at a concentration of 0.01 to 0.05 g/dl and the sugar alcohols at a concentration of 1 to 20 g/dl. When aspartame is used at a concentration less than 0.01 g/dl, the desired effects of the present invention may not be attained, depending on the kinds and concentrations of other ingredients contained therein.
The combined use of aspartame, sorbitol, maltitol and "other oligosugar alcohols" in particular ratios according to the present invention makes it possible to markedly improve the quality of the sweetness of aspartame, in comparison with the cases where those sugar alcohols are used individually, or in comparison with known sweetening agents or combinations of sweetening agents. Accordingly, there can be provided by the present invention a sweetener or a sweetened food having a sweetness which is very similar to that of sucrose with regard to initial taste, richness, sustainability and aftertaste.
The present invention will further be illustrated by examples.
Sample solutions shown in Table 1 were prepared and subjected to a sensory test of a panel of 15 members in accordance with the two point comparison method, using an aqueous 10 g/dl sucrose solution as a control. Results obtained are shown in Table 2. The quality of the sweetness of aspartame could be markedly improved in samples (in particular, in Sample 5) comprising all the three ingredients (sorbitol, maltitol and "other oligosugar alcohols"), whereas little effects could be attained in cases where only one or two of said three ingredients were employed.
TABLE 1
__________________________________________________________________________
Other Oligo-
Sample
Aspartame
Sorbitol
Maltitol
Alcohols
HG.sub.1 :HG.sub.2 :≧HG.sub.3
[AP]/[HG.sub.1 + HG.sub.2
+ ≧HG.sub.3 ]
No. (AP) (HG.sub.1)
(HG.sub.2)
(≧HG.sub.3)
(Weight Ratio)
(Ratio of Sweetness)
__________________________________________________________________________
1 0.030 g/dl
6.7 g/dl
-- -- 1:0:0 6/4
2 0.030 g/dl
-- 5.0 g/dl
-- 0:1:0 6/4
3 0.030 g/dl
-- -- 26.7 g/dl
0:0:1 6/4
4 0.030 g/dl
0.84 g/dl
1.68 g/dl
14.3 g/dl
5:10:85 6/4
5 0.030 g/dl
0.25 g/dl
4.1 g/dl
3.85 g/dl
3:50:47 6/4
6 0.0475 g/dl
0.03 g/dl
0.51 g/dl
0.48 g/dl
3:50:47 9.5/0.5
7 0.050 g/dl
-- -- -- -- 10/0
__________________________________________________________________________
Notes:
The sample solutions were so adjusted that they have a sweetness
corresponding to an aqueous 10 g/dl sucrose solution.
Sorbitol (HG.sub.1) had a sweetness 0.6 times that of sucrose; maltitol
(HG.sub.2), 0.8 times that of sucrose; and "other oligosugar alcohols
(≧HG.sub.3)", 0.15 times that of sucrose.
TABLE 2
______________________________________
Sample
Initial*.sup.1
Richness of*.sup.1 Overall*.sup.2
No. Sweetness Sweetness Aftertaste*.sup.1
Rating
______________________________________
1 -0.4 -2.0 +1.4 4.6
2 -1.4 -1.8 +1.4 4.2
3 -1.6 -1.4 +1.2 4.8
4 -0.6 -1.2 +1.4 5.0
5 +0.4 +0.2 -0.8 7.4
6 -1.6 -2.4 +1.4 5.4
7 -1.8 -2.2 +1.6 4.4
______________________________________
*.sup.1 Rating Used:
+3 -- Considerably strong
+2 -- Fairly Strong
+3 -- Slightly strong
0 -- Equal to sucrose
-1 -- Slightly weak
-2 -- Fairly weak
-3 -- Considerably weak
*.sup.2 Rating Used:
10 -- Best
5 -- Average
0 -- Poor
The overall rating of the aqueous sucrose solution was 7.2. The "other oligosugar alcohols (HG3 and above)" used in the above test was obtained by reducing dextrin having a DE value of about 20 and then recovering fractions of HG3 and above by column chromatography.
______________________________________
Conditions of Column Chromatography:
______________________________________
Gel used Toyo Pearl HW-40S by Toyo Soda Mfg. Co.
Eluent H.sub.2 O
Rate of elution
ca. 40 ml/Hr
Temperature
ca. 50° C.
______________________________________
The composition of the oligosugar alcohols recovered by the column chromatography was analysed by high pressure liquid chromatography (HPLC). The following results were obtained: Content of HG3 to HG9 components, 72%; and content of the components of HG10 and above, 28%.
______________________________________
Conditions of HPLC
______________________________________
Gel used Aminex HPX-87C by Bio Rad Co.
Eluent H.sub.2 O
Rate of elution
ca. 0.6 ml/min.
Temperature ca. 85° C.
______________________________________
Three kinds of carbonated lemon lime beverages were prepared using ingredients shown in Table 3.
TABLE 3
______________________________________
Product
of the Control Control
Ingredients Invention Sample 1 Sample 2
______________________________________
Sucrose -- 100 g --
Aspartame 0.3 -- 0.5
Sorbitol 2.5 -- --
Maltitol 41.0 -- --
Oligosugar alcohols
38.5 -- --
(HG.sub.3 and above)
Citric acid 1.25 1.25 1.25
Sodium Citrate
0.5 0.5 0.5
Lemon Lime 1.0 1.0 1.0
Essence
Carbonated Water
(Up to a total volume of 1 liter)
______________________________________
The carbonated lemon lime beverages obtained were evaluated by a sensory test performed by a panel of 10 members in accordance with the two point comparison method, using Control Sample 1 (sucrose-containing sample) as a control. Results obtained are shown in Table 4.
TABLE 4
______________________________________
Initial Richness of Overall
Sample Sweetness Sweetness Aftertaste
Rating
______________________________________
Product +0.2 +0.2 -0.2 7.2
of the
Invention
Control -1.5 -2.0 +1.8 4.8
Sample 1
Control 0 0 0 7.0
Sample 1
______________________________________
The beverages obtained were evaluated by the same rating as in Experiment (Table 2) described hereinabove. It will be recognized that the quality of the sweetness of aspartame could be markedly improved by the combined used of the three ingredients: sorbitol, maltitol and oligosugar alcohols (HG3 and above).
TABLE 5
______________________________________
Product of Control
Ingredients the Invention
Sample
______________________________________
Aspartame 1.8 1.9
Sorbitol 3.0 --
Maltitol 49.1 98.1
Oligosugar alcohols
46.1 --
(HG.sub.3 and above)
______________________________________
Granules of table sweeteners (moisture content: less than 1%) were prepared from the ingredients shown in Table 5, thereby using water as a binder. The product according to the invention had a sweetness degree of 4 (i.e., the sweetness of 1 g of the product according to the invention corresponded to that of 4 g of sucrose). The two kinds of sugar granules obtained were separately added to coffee, tea, and plain yoghurt in an amount of 1.5 g/100 ml each and evaluated by a sensory test of a panel of 15 members using sucrose as a control. Results obtained are shown in Table 6.
TABLE 6
______________________________________
Initial Richness of Overall
Sample Sweetness Sweetness Aftertaste
Rating
______________________________________
Coffee
Product of
+0.4 +0.2 -1.2 7.4
the Invention
Control -1.6 -1.4 -0.8 5.2
Sample
Tea
Product of
+0.6 +0.8 -0.4 6.8
the Invention
Control -1.2 -1.6 +1.6 4.8
Sample
Plain
Yoghurt
Product of
+0.2 +0.4 -0.2 7.2
the Invention
Control -0.4 -0.2 +0.2 5.6
Sample
______________________________________
The samples were evaluated by the same rating as in Experiment (Table 2). It will be understood that the quality of the sweetness of aspartame could be markedly improved by using aspartame in combination with the three ingredients: sorbitol, maltitol and oligosugar alcohols (HG3 and above).
In cases where aspartame is to be used as a sweetener, in particular as a liquid sweetener, the sugar alcohols according to the present invention can be heated before being admixed with aspartame. Such a liquid sweetener is capable of maintaining a high concentration of aspartame even after being cooled to room temperature and, therefore, possesses a strong sweetness of superior quality. In such a case, the sugar alcohols can be preheated to a temperature of 50° to 110° C., preferably 60° to 90° C. When the temperature is lower than 50° C., part of aspartame may remain undissolved, and when it is above 110° C., decomposition of aspartame may take place. The concentration of aspartame in said liquid sweetener can be preferably from 0.3% by weight (degree of sweetness: ca. 1.0) to 0.8% by weight (degree of sweetness: ca. 2.0). When it is less than 0.3% by weight, there may be caused diarrhea, and when it is more than 0.8% by weight, an inferior quality of sweetness may result.
In order to further improve its quality of sweetness, the sweetener or sweetened food of the present invention can be additionally incorporated with sodium salts of organic acids, such as sodium tartrate, sodium malate and sodium citrate. Such organic acid salts can be used in an amount of from 30 to 300% by weight, preferably from 30 to 200% by weight. When the quality of sweetness of the solutions containing 0.05 g of aspartame and 0.05 g or 0.0002 mol/dl of sodium salts of three organic acids were organoleptically evaluated by a panel of 12 members, sodium tartrate received the highest mark, followed by sodium malate.
TABLE 7
______________________________________
Product
of the Control Control
Ingredients Invention Sample 1 Sample 2
______________________________________
Sucrose -- 115.0 g --
Aspartame 0.40 g -- 0.56 g
Sorbitol (HG.sub.1)
1.0 -- --
Maltitol (HG.sub.2)
13.0 -- --
Other/Oligo-
11.0 -- --
sugar alcohols
(HG.sub.3 and above)
Citric Acid 2.4 2.4 g 2.4
Sodium Citrate
0.5 0.5 0.5
Vitamin C 0.2 0.2 0.2
Concentrated
20.0 20.0 20.0
Orange Juice (1/5)
Orange Essence
1.0 1.0 1.0
Water (Up to a total weight of 1,000 g)
______________________________________
Three kinds of juice-containing beverages were prepared from the ingredients shown in Table 7. The beverages obtained were organoleptically evaluated by a panel of 20 members in accordance with the two point comparison method, using Control Sample 1 (sucrose-containing sample) as a control. Results obtained are shown in Table 8.
TABLE 8
______________________________________
Initial Richness of Overall
Sample Sweetness Sweetness Aftertaste
Rating
______________________________________
Product -0.2 -0.2 -0.6 5.8
of the
Invention
Control -1.2 -1.8 +0.8 4.8
Sample 2
Control 0 0 0 5.6
Sample 1
______________________________________
(In this test was used the same rating as in EXPERIMENT)
It can be seen that the quality of the sweetness of aspartame could be improved by using it in combination with sorbitol, maltitol and the "other oligosugar alcohols" (HG3 and above).
A liquid sweetener (A) was prepared from the following ingredients.
______________________________________ Sugar alcohols* 100 g Aspartame 0.35 g Sodium tartrate 0.4 g ______________________________________ [Note *A mixture of sorbitol:maltitol:"other oligo alcohols" = 3:50:45 (based o weight)
In the above preparation, the sugar alcohols were heated to about 80° C. and admixed with aspartame and sodium tartrate by using a mixer.
The thus obtained liquid sweetener was clear. When added to coffee and tea, the sweetener was capable of imparting a satisfactory sweetness to both of them.
______________________________________ Sugar alcohols* 100 g Aspartame 0.85 g Sodium Tartrate 0.6 g ______________________________________ [Note *A mixture of sugar alcohols having the same composition as the one used in Example 4.
A liquid sweetner (B) was prepared from the above ingredients in the same manner as in Example 4, except that the sugar alcohols were heated to a temperature of about 90° C. before being admixed. When this sweetener was allowed to stand at room temperature, there was formed a small amount of precipitate or gel of aspartame. However, it was usable as a liquid sweetener in either case. When added to coffee, the sweetener gave a satisfactory sweetness to the coffee as in the case of Example 4.
Claims (1)
1. A sweetener for foods, which comprises aspartame, in combination with:
1-10 wt.% sorbitol,
45-55 wt.% maltitol, and
35-55 wt.% of fractions obtained by reducing dextrin, said fractions having 3 or more sugar units,
wherein said wt.%'s are each based on the combined weight of said sorbitol, maltitol and said fractions obtained by reducing dextrin,
wherein aspartame is contained in an amount such that the weight ratio of the combined sweetness of said sorbitol, maltitol and fractions obtained by reducing dextrin to the sweetness of said aspartame is 0.5:9.5 to 3:7, wherein the sweetness corresponds to an aqueous 10 g/dl sucrose solution.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61-66179 | 1986-03-25 | ||
| JP6617986 | 1986-03-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4770889A true US4770889A (en) | 1988-09-13 |
Family
ID=13308359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/026,306 Expired - Fee Related US4770889A (en) | 1986-03-25 | 1987-03-16 | Sweetener |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US4770889A (en) |
| JP (1) | JPH0732686B2 (en) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4888183A (en) * | 1987-07-28 | 1989-12-19 | Mitsubishi Kasei Corporation | Fermented milk |
| US4970083A (en) * | 1988-10-04 | 1990-11-13 | Kabushiki Kaisha Yakult Honsha | Lactic acid fermented food and method of manufacturing the same |
| US5080916A (en) * | 1987-12-28 | 1992-01-14 | Mitsubishi Kasei Corporation | Low-caloric sweetening composition of microcrystalline appearance |
| US5637334A (en) * | 1993-09-30 | 1997-06-10 | Wm. Wrigley Jr. Company | Chewing gum containing maltitol |
| US5736185A (en) * | 1995-08-21 | 1998-04-07 | Nikken Chemicals Co., Ltd. | Method for suppressing grassy smell and acid taste of vegetables and fruit |
| US6126981A (en) * | 1994-06-30 | 2000-10-03 | Kraft Foods, Inc. | Ready-to-drink, aspartame-sweetened beverages |
| US20020160090A1 (en) * | 2001-04-27 | 2002-10-31 | Pepsico, Inc. | Use of erythritol and D-tagatose in diet or reduced-calorie beverages and food products |
| US20020197371A1 (en) * | 2001-04-27 | 2002-12-26 | Pepsico, Inc. | Use of erythritol and D-tagatose in zero-or low-calorie beverages and food products |
| US20050196503A1 (en) * | 2004-03-05 | 2005-09-08 | Sunil Srivastava | High-intensity sweetener-polyol compositions |
| US20070082106A1 (en) * | 2001-04-27 | 2007-04-12 | Thomas Lee | Use of Erythritol and D-Tagatose In Diet or Reduced-Calorie Beverages and Food Products |
| US20070271944A1 (en) * | 2005-12-02 | 2007-11-29 | Coca-Cola Company | Reduced calorie frozen beverage |
| US8017168B2 (en) | 2006-11-02 | 2011-09-13 | The Coca-Cola Company | High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith |
| US8465786B2 (en) * | 2001-04-20 | 2013-06-18 | The Coca-Cola Company | Non caloric frozen carbonated beverage |
| US9101160B2 (en) | 2005-11-23 | 2015-08-11 | The Coca-Cola Company | Condiments with high-potency sweetener |
| US20230157338A1 (en) * | 2018-05-20 | 2023-05-25 | Todd Ewing | Electrolyte-enhanced sweetener and consumable products obtained |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008018643A1 (en) | 2006-08-11 | 2008-02-14 | Ajinomoto Co., Inc. | Carbonated beverage and method of producing carbonated beverage |
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| US4208431A (en) * | 1978-05-05 | 1980-06-17 | Life Savers, Inc. | Long-lasting chewing gum having good processibility and method |
| US4346116A (en) * | 1978-12-11 | 1982-08-24 | Roquette Freres | Non-cariogenic hydrogenated starch hydrolysate, process for the preparation and applications of this hydrolysate |
| US4357354A (en) * | 1980-11-25 | 1982-11-02 | Nabisco Brands, Inc. | Reduced calorie chewing gum |
| US4374858A (en) * | 1979-10-04 | 1983-02-22 | Warner-Lambert Company | Aspartame sweetened chewing gum of improved sweetness stability |
| US4497846A (en) * | 1982-04-30 | 1985-02-05 | Roquette Freres | Sugarless hard candy |
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| US4597970A (en) * | 1984-10-05 | 1986-07-01 | Warner-Lambert Company | Chewing gum compositions containing novel sweetener delivery systems and method of preparation |
| US4722844A (en) * | 1982-08-17 | 1988-02-02 | Ajinomoto Co., Inc. | Process of stabilizing aspartame sweetness in water-containing foods |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57155965A (en) * | 1981-03-19 | 1982-09-27 | Ajinomoto Co Inc | Low-calorie sweetening composition |
| JPS58116633A (en) * | 1981-12-29 | 1983-07-11 | Ajinomoto Co Inc | Preparation of sugarless candy with starch base or candy with starch base having reduced amount of sugar |
| JPS60149358A (en) * | 1984-01-11 | 1985-08-06 | Meiji Seika Kaisha Ltd | Sweetening mix |
| FR2559033B1 (en) * | 1984-02-07 | 1987-03-27 | Roquette Freres | SUGAR-FREE ICE CREAM AND ITS PREPARATION METHOD |
-
1987
- 1987-03-16 US US07/026,306 patent/US4770889A/en not_active Expired - Fee Related
- 1987-03-16 JP JP62060450A patent/JPH0732686B2/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4208431A (en) * | 1978-05-05 | 1980-06-17 | Life Savers, Inc. | Long-lasting chewing gum having good processibility and method |
| US4346116A (en) * | 1978-12-11 | 1982-08-24 | Roquette Freres | Non-cariogenic hydrogenated starch hydrolysate, process for the preparation and applications of this hydrolysate |
| US4374858A (en) * | 1979-10-04 | 1983-02-22 | Warner-Lambert Company | Aspartame sweetened chewing gum of improved sweetness stability |
| US4357354A (en) * | 1980-11-25 | 1982-11-02 | Nabisco Brands, Inc. | Reduced calorie chewing gum |
| US4497846A (en) * | 1982-04-30 | 1985-02-05 | Roquette Freres | Sugarless hard candy |
| US4722844A (en) * | 1982-08-17 | 1988-02-02 | Ajinomoto Co., Inc. | Process of stabilizing aspartame sweetness in water-containing foods |
| US4556565A (en) * | 1983-11-04 | 1985-12-03 | Tetsuo Arima | Sweetener composition, process for making the same, and comestibles comprising said sweetener composition |
| US4597970A (en) * | 1984-10-05 | 1986-07-01 | Warner-Lambert Company | Chewing gum compositions containing novel sweetener delivery systems and method of preparation |
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4888183A (en) * | 1987-07-28 | 1989-12-19 | Mitsubishi Kasei Corporation | Fermented milk |
| US5080916A (en) * | 1987-12-28 | 1992-01-14 | Mitsubishi Kasei Corporation | Low-caloric sweetening composition of microcrystalline appearance |
| US4970083A (en) * | 1988-10-04 | 1990-11-13 | Kabushiki Kaisha Yakult Honsha | Lactic acid fermented food and method of manufacturing the same |
| US5637334A (en) * | 1993-09-30 | 1997-06-10 | Wm. Wrigley Jr. Company | Chewing gum containing maltitol |
| US6126981A (en) * | 1994-06-30 | 2000-10-03 | Kraft Foods, Inc. | Ready-to-drink, aspartame-sweetened beverages |
| US5736185A (en) * | 1995-08-21 | 1998-04-07 | Nikken Chemicals Co., Ltd. | Method for suppressing grassy smell and acid taste of vegetables and fruit |
| US8465786B2 (en) * | 2001-04-20 | 2013-06-18 | The Coca-Cola Company | Non caloric frozen carbonated beverage |
| US20060068072A9 (en) * | 2001-04-27 | 2006-03-30 | Pepsico, Inc. | Use of erythritol and D-tagatose in diet or reduced-calorie beverages |
| US7579032B2 (en) | 2001-04-27 | 2009-08-25 | Pepsico, Inc. | Use of erythritol and D-tagatose in zero-or low-calorie beverages |
| US20020160090A1 (en) * | 2001-04-27 | 2002-10-31 | Pepsico, Inc. | Use of erythritol and D-tagatose in diet or reduced-calorie beverages and food products |
| US20020197371A1 (en) * | 2001-04-27 | 2002-12-26 | Pepsico, Inc. | Use of erythritol and D-tagatose in zero-or low-calorie beverages and food products |
| US20070082106A1 (en) * | 2001-04-27 | 2007-04-12 | Thomas Lee | Use of Erythritol and D-Tagatose In Diet or Reduced-Calorie Beverages and Food Products |
| US7815956B2 (en) | 2001-04-27 | 2010-10-19 | Pepsico | Use of erythritol and D-tagatose in diet or reduced-calorie beverages and food products |
| US20090280232A1 (en) * | 2001-05-01 | 2009-11-12 | Pepsico., Inc. | Use Of Erythritol And D-Tagatose In Zero- Or Low-Calorie Beverages |
| US8221815B2 (en) | 2001-05-01 | 2012-07-17 | Pepsico, Inc. | Use of erythritol and D-tagatose in zero- or low-calorie beverages |
| US20050196503A1 (en) * | 2004-03-05 | 2005-09-08 | Sunil Srivastava | High-intensity sweetener-polyol compositions |
| WO2005087020A1 (en) * | 2004-03-05 | 2005-09-22 | Richmond Chemical Corporation | High-intensity sweetener-polyol compositions |
| US9101160B2 (en) | 2005-11-23 | 2015-08-11 | The Coca-Cola Company | Condiments with high-potency sweetener |
| US20070271944A1 (en) * | 2005-12-02 | 2007-11-29 | Coca-Cola Company | Reduced calorie frozen beverage |
| US8017168B2 (en) | 2006-11-02 | 2011-09-13 | The Coca-Cola Company | High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith |
| US20230157338A1 (en) * | 2018-05-20 | 2023-05-25 | Todd Ewing | Electrolyte-enhanced sweetener and consumable products obtained |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0732686B2 (en) | 1995-04-12 |
| JPS6312263A (en) | 1988-01-19 |
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